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5 дней назад

Senior Clinical Research Associate II (Medical)

217 500PLN
Формат работы
remote (только Poland)
Тип работы
fulltime
Грейд
senior
Английский
b2
Страна
Poland
Вакансия из списка Hirify.GlobalВакансия из Hirify Global, списка международных tech-компаний
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Мэтч & Сопровод

Для мэтча с этой вакансией нужен Plus

Описание вакансии

Текст:
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TL;DR
Senior Clinical Research Associate II (Medical): Managing and monitoring investigator sites for clinical trials from site initiation through database lock and close-out with an accent on patient safety, GCP compliance, and site quality. Focus on resolving protocol and data issues, supporting recruitment and database release, overseeing investigational products, and mentoring clinical research associates.

Location: Remote in Poland

Salary: Minimum annual gross base salary of 217,500 PLN; annual bonus of 15%

Company

hirify.global develops medicines and clinical solutions focused on improving patient health outcomes.

What you will do

  • Manage and monitor assigned investigator sites from site initiation through database lock and study close-out.
  • Ensure clinical trials follow monitoring plans, applicable laws, Good Clinical Practice, and hirify.global standards.
  • Serve as the primary contact for investigator sites, coordinating with Site Care Partners, study teams, vendors, and investigators.
  • Support site activation, patient recruitment, protocol training, safety reporting, data-query resolution, and database release.
  • Oversee investigational product receipt, handling, storage, accounting, and destruction at investigator sites.
  • Mentor Clinical Research Associates, act as a subject-matter expert for CRA processes, and participate in process-improvement initiatives.

Requirements

  • Experience managing investigator sites and conducting onsite, remote, or electronic clinical trial monitoring.
  • Thorough knowledge of the assigned product, protocol, therapy area, patient safety, and clinical monitoring risks.
  • Ability to resolve protocol deviations, data queries, corrective and preventive actions, audit observations, and site-level issues within required timelines.
  • Ability to collaborate with investigators, healthcare professionals, study clinicians, Site Care Partners, study teams, vendors, and drug-safety specialists.
  • Must be based in Poland for the remote role.

Culture & Benefits

  • Patient-centric work guided by courage, joy, equity, and excellence.
  • Flexible workplace culture supporting work-life harmony.
  • Corporate benefits including Medicover, Multisport, life insurance, and a private pension plan.
  • Inclusive workplace with reasonable adjustments available during recruitment and employment.

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